U.S. Laser Worx Patriot 1 family of lasers— 510(k) K162334

Substantially Equivalent

U.S. Laser Worx

FDA 510(k) clearance K162334 for U.S. Laser Worx Patriot 1 family of lasers, Substantially Equivalent on 2017-04-27. Applicant: U.S. Laser Worx.

Clearance details

Applicant
U.S. Laser Worx
Product code
Code GEX
Advisory panel
General, Plastic Surgery
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
San Antonio, TX, US
Download summary PDFView on FDA.gov ↗

Adverse events under product code GEX

product code GEX
Death
33
Injury
3,045
Malfunction
12,903
Other
25
Total
16,006

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.